A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613299



Internal ID16400708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8903857..9032105hg38UCSC Ensembl
Innerchr9:8903857..9032105hg19UCSC Ensembl
Innerchr9:8893857..9022105hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38128249
hg19128249
hg18128249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126893
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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